Morphology of gas‐assisted and conventional injection molded polycarbonate/polyethylene blend

The skin‐core structure of the gas‐assisted and conventional injection molded polycarbonate (PC)/polyethylene (PE) blend was investigated. The results indicated that both the size and the shape of the dispersed PC phase depended not only on the nature of PC/PE blend and molding parameters, but also on its location in the parts. Although the gas‐assisted injection molding (GAIM) parts and conventional injection molding (CIM) part have the similar skin‐core structure, the morphology evolution of PC phase in the GAIM moldings and the CIM moldings showed completely different characteristics. In the section perpendicular to the melt flow direction, the morphology of the GAIM moldings included five layers, skin intermediate layer, subskin, core layer, core intermediate layer as well as gas channel intermediate layer, according to the degree of deformation. PC phase changed severely in the core layer of GAIM moldings, as well as in the subskin of CIM moldings. In GAIM parts, PC phase in the core layer of the nongate end changed far more intensely and aligned much orderly than that in the gate end. The morphology of PC phase in the GAIM part molded with higher gas pressure changed more severe than that in the GAIM part molded with lower gas pressure. In a word, PC phase showed more obvious fibrillation in the GAIM moldings than that in the CIM moldings. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 3069–3077, 2006     

Hierarchic structure and mechanical property of glass fiber reinforced isotactic polypropylene composites molded by multiflow vibration injection molding

Maleic anhydride‐grafted polypropylene (Ma‐PP) and β nucleation agents (β‐NA) were used to modify the glass fiber (GF)/isotactic polypropylene (iPP) composite. The interface adhesion, degree of orientation, and crystalline morphologies of the PP/GF composites molded by multiflow vibrate‐injection molding (MFVIM) and conventional injection molding (CIM) were studied by polarized light microscopy (PLM), scanning electronic microscopy (SEM), and X‐ray measurements. Results prove that the interface adhesion was improved by the Ma‐PP; γ crystal was generated by the MFVIM due to the instant high pressure and shear during the multiflow; and a hierarchical structure which has a strengthened skin and a toughened core was formed. As a result, the final PP/GF/β‐NA composite has a 60% increase in tensile strength and 80% improvement in impact strength compare with the CIM pure PP/GF composite. Based on the observations, a modified model is proposed to interpret the strengthening and toughening mechanism. Our work paves the way to obtain high‐performance GF/iPP composites. POLYM. COMPOS., 38:2707–2717, 2017. © 2015 Society of Plastics Engineers     

流动场下含β成核剂的玻璃纤维增强聚丙烯复合材料结构与性能研究

采用普通注射成型和动态保压注射成型分别制备了不同玻璃纤维（GF）含量和β成核剂含量的等规聚丙烯（iPP）复合材料,测试了复合材料的力学性能,并采用二维广角X射线衍射、扫描电子显微镜和二维小角X射线散射研究了复合材料的iPP分子链取向、GF取向及结晶性能。结果表明,在动态保压注射成型条件下,GF含量为30 %（质量分数,下同）、β成核剂含量为0.2 %时,复合材料具有最优异的综合性能,拉伸强度为58.52 MPa,冲击强度为9.26 kJ/m2,这是由于在流动场下含GF与β成核剂的复合材料形成了"皮刚芯韧"类竹子的仿生结构。     

气辅注射成型玻璃纤维增强聚丙烯的发泡结构

用扫描电镜对气辅注射成型玻璃纤维(GF)增强聚丙烯(PP)制品横截面进行观察.结果表明,在靠近气道内壁一定厚度的区域内都有发泡结构生成,而纯PP的气辅注射成型制品则没有这种发泡结构,并且这种发泡程度一般随着GF含量和气体压力的增加而增大;在形貌分析的基础上,探讨了气辅注射成型过程中GF和气体穿透对发泡结构形成的影响.     

微发泡PP/GF复合材料力学性能研究

采用化学发泡注塑成型的方法制备了微发泡聚丙烯/玻璃纤维(PP/GF)复合材料;结合成核理论和玻纤增强机理,研究了发泡质量对微发泡PP/GF复合材料力学性能的影响。结果表明:在PP/GF复合材料中添加5.0%纳米SiO2后,纳米SiO2对PP与GF的相容性并无太大影响,微孔发泡PP/GF复合材料的拉伸强度和冲击强度得到较大提高。     

动态注射成型短玻纤增强高密度聚乙烯力学性能的研究

在不同的振动条件下注射成型短玻纤增强高密度聚乙烯复合材料。实验表明,振动可以有效地改善玻纤在树脂基体中的分散取向状况,提高复合材料的力学性能。与稳态注射成型的复合材料相比,动态注射成型复合材料的拉伸强度最大可提高11.1%,冲击强度最大可提高11.4%。     

Gas‐assisted injection molded polypropylene: The skin‐core structure

In this article, gas penetration‐induced skin‐core structure of isotactic polypropylene(iPP), which is molded by gas‐assisted injection molding at different gas pressures, was investigated. For comparison, the counterpart was also molded by conventional injection molding (CIM) using the same processing parameters but without gas penetration. They were characterized via PLM, DSC, and SEM. And the crystal morphology at different gas pressures was principally concerned. For the GAIM parts, highly oriented structure is formed in the skin zone, and much less oriented structure in the inner zone (near the gas channel surface). Furthermore, it is suggested that the naked shish structure can be developed in the skin zone of GAIM part, which is molded at higher gas pressures, and shish‐kebab structure is mainly formed in the skin zone of that, which is molded at lower gas pressure. However, for the CIM part, from the skin to the core zone, the dominant morphological feature is spherulite. In a word, the presence of gas penetration notably enhances the oriented structure formation and gives rise to the skin‐core structure. POLYM. ENG. SCI., 2008. © 2008 Society of Plastics Engineers     

Experiment and simulation of foaming injection molding of polypropylene/nano-calcium carbonate composites by supercritical carbon dioxide

Microcellular injection molding of neat isotactic polypropylene (iPP) and isotactic polypropylene/nano-calcium carbonate composites (iPP/nano-CaCO₃H) was performed using supercritical carbon dioxide as the physical blowing agent. The influences of filler content and operating conditions on microstructure morphology of iPP and iPP/nano-CaCO₃H microcellular samples were studied systematically. The results showed the bubble size of the microcellular samples could be effectively decreased while the cell density increased for iPP/nano-CaCO₃H composites, especially at high CO₂ concentration and back pressure, low mold temperature and injection speed, and high filler content. Then Moldex 3D was applied to simulate the microcellular injection molding process, with the application of the measured ScCO₂ solubility and diffusion data for iPP and iPP/nano-CaCO₃H composites respectively. For neat iPP, the simulated bubble size and density distribution in the center section of tensile bars showed a good agreement with the experimental values. However, for iPP/nano-CaCO₃H composites, the correction factor for nucleation activation energy F and the pre-exponential factor of nucleation rate f0 were obtained by nonlinear regression on the experimental bubble size and density distribution. The parameters F and f0 can be used to predict the microcellular injection molding process for iPP/nano-CaCO₃H composites by Moldex 3D.     

Biaxial self‐reinforcement of isotactic polypropylene prepared in uniaxial oscillating stress field by injection molding. I. Processing conditions and mechanical properties

This research explores the longitudinal and latitudinal mechanical properties of injection‐molded isotactic polypropylene (iPP) prepared in a uniaxial oscillating stress field by oscillating packing injection molding (OPIM). The methods, processing conditions, and mechanical test results for iPP by conventional injection molding (CIM) and OPIM are described. The mechanical properties in the flow direction (MD) and transverse direction (TD) of the OPIM moldings indicate three types of self‐reinforced iPP moldings. The pronounced biaxially self‐reinforced iPP specimens exhibit a 55–70% increase of the tensile strength and more than a fourfold increase of the impact strength in the MD, together with more than a 40% increase of the tensile strength and a 30–40% increase of the impact strength in the TD. The OPIM moldings show different stress–strain behavior in the MD and TD. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 78: 1906–1910, 2000     

Enhanced β‐crystal formation of isotactic polypropylene under the combined effects of acid‐corroded glass fiber and preshear

The acid‐corroded glass fiber (GF)/isotactic polypropylene (iPP) composite was injection molded by mixing–injection molding (MIM). Through this method, preshear can be imposed on melt during mix–plasticization process. The crystalline structure across the thickness direction of the injection‐molded bars was investigated by wide‐angle X‐ray diffraction and differential scanning calorimetry (DSC). It was unexpectedly found that, in core region, the acid‐corroded GF/iPP sample has the highest content of β‐form crystals, followed by uncorroded GF/iPP and neat iPP. Additionally, the crystalline morphology was investigated by polarized optical microscopy (POM) and scanning electron microscopy, and the results showed that β‐transcrystallization is preferably present in the acid‐corroded GF/iPP system. Confirmed by POM and DSC, the acid‐corroded GF shows strong β‐nucleation ability to iPP under static condition. Combined with the main features of MIM, three β‐nucleation origins in the acid‐corroded GF/iPP system under injection molding condition are proposed: (1) precursors induced by preshear in the barrel, (2) row‐nuclei induced by local shear, and (3) the acid‐corroded GF nuclei. POLYM. COMPOS. 34:1250–1260, 2013. © 2013 Society of Plastics Engineers     

Linear viscoelastic and morphological description of multiphase systems affected by processing parameters

Influence of processing methods, in terms of comparing compression and injection moldings, on the rheological behavior of polycarbonate (PC)/acrylonitrile‐butadiene‐styrene (ABS) blends and PC/ABS/glass fibers composites is presented. Blend compositions and fiber content are considered as material variables. For blends, the effect of the processing route on the viscoelastic functions is evident only for low shearing frequencies. Injection molding created morphology with cocontinuous character, while compression molded blends have “relaxed” structure, where dispersed phase domains are several times larger than in injection molded ones. The glass fiber reinforcement led to the significant differences in viscoelastic properties of composites processed by injection and compression molding. Injected composites have both moduli always higher than compression molded. Also, fiber lengths are reduced more for compressing molding. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

The morphology and property of HDPE in the presence of oscillation pressure and poly(ethylene terephthalate)

The injection‐molded specimens of neat HDPE and the PET/HDPE blends were prepared by conventional injection molding (CIM) and by pressure vibration injection molding (PVIM), respectively. The effect of oscillation pressure and PET phase with different shapes on superstructure and its crystal orientation distribution of injection molded samples were characterized by differential scanning calorimetry (DSC), scanning electron microscopy (SEM), and two‐dimension wide‐angle X‐ray diffraction techniques (2D‐WAXD). Hermans' orientation functions were determined from the wide‐angle X‐ray diffraction patterns. With the PET particles added, the shear viscosity of blend increase and crystallization rate of HDPE phase is enhanced. For the neat HDPE samples, with the promotion from oscillation shear, the orientation parameter experienced a large increase, moreover, the PVIM can induce transverse lamellae (kebabs) twisting in growth direction. Because of the redefined flow field and nucleation effect of PET particles, the crystal orientation of blend is also increased. So the tensile strength of vibration samples enhanced and elongation at break declined. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Mechanical properties and morphology of polypropylene‐calcium carbonate nanocomposites prepared by dynamic packing injection molding

In this article, dynamic packing injection molding (DPIM) technology was used to prepare injection samples of Polypropylene‐Calcium Carbonate (PP/CaCO₃) nanocomposites. Through DPIM, the mechanical properties of PP/nano‐CaCO₃ samples were improved significantly. Compared with conventional injection molding (CIM), the enhancement of the tensile strength and impact strength of the samples molded by DPIM was 39 and 144%, respectively. In addition, the tensile strength and impact strength of the PP/nano‐CaCO₃ composites molded by DPIM increase by 21 and 514%, respectively compared with those of pure PP through CIM. According to the SEM, WAXD, DSC measurement, it could be found that a much better dispersion of nano‐CaCO₃ in samples was achieved by DPIM. Moreover, γcrystal is found in the shear layer of the DPIM samples. The crystallinity of PP matrix in DPIM sample increases by 22.76% compared with that of conventional sample. The improvement of mechanical properties of PP/nano‐CaCO₃ composites prepared by DPIM attributes to the even distribution of nano‐CaCO₃ particles and the morphology change of PP matrix under the influence of dynamic shear stress. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Hierarchical crystalline structure of HDPE molded by gas-assisted injection molding

To understand the crystalline morphology of the parts molded by gas-assisted injection molding (GAIM), in this work, the hierarchical structures and the crystalline morphology of gas-assisted injection molded high-density polyethylene (HDPE) were investigated. According to the comparison between the results of the GAIM part and those of the conventional injection molded counterpart, it is found that gas penetration can remarkably enhance the shear rate during GAIM process and oriented lamellar structure, shish-kebab structure and common spherulites arise in the skin, subskin and gas channel region, respectively, owing to the different shear rate in these regions. Meanwhile, cooling rate also plays an important role in the formation of the oriented crystalline structure.     

Properties of glass‐filled thermoplastic polyesters

The thermal, mechanical, and rheological properties of glass‐filled poly(propylene terephthalate) (GF PPT) were compared to glass‐filled poly(butylene terephthalate) (GF PBT). The impetus for this study was the recent commercial interest in PPT as a new glass‐reinforced thermoplastic for injection‐molding applications. This article represents the first systematic comparison of the properties of GF PPT and GF PBT in which differences in properties can be attributed solely to differences in the polyester matrices, that is, glass‐fiber size and composition, polymer melt viscosity, nucleant content and composition, polymerization catalyst composition and content, and processing conditions were kept constant. Under these controlled conditions, GF PPT showed marginally higher tensile and flexural properties and significantly lower impact strength compared to GF PBT. The crystallization behavior observed by cooling from the melt at a constant rate showed that GF PBT crystallized significantly faster than did GF PPT. Nucleation of GF PPT with either talc or sodium stearate increased the rate of crystallization, but not to the level of GF PBT. The slower crystallization rate of GF PPT was found to strongly affect thermomechanical properties of injection‐molded specimens. For example, increasing the polymer molecular weight and decreasing the mold temperature significantly increased the modulus drop associated with the glass transition. In contrast, the modulus–temperature response of GF PBT was just marginally influenced by the polymer molecular weight and was essentially independent of the mold temperature. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 74: 889–899, 1999     

粉末浸渍长玻璃纤维增强聚丙烯的注塑

采用粉末浸渍的方法制备连续玻璃纤维增强聚丙烯预浸料,经切割获得长纤维增强聚丙烯粒子,探索了材料的注塑工艺,研究了注塑后材料的力学性能及其影响因素。结果表明,粉末浸渍的长纤维增强聚丙烯经注塑后可获得力学性能的制品;随着预浸料切割长度的增长、纤维含量的增加,材料的力学性能提高;在基体聚丙烯中添加接枝极性基团的功能化聚丙烯,可改善体系的界面结合,提高材料的力学性能,但功能化聚丙烯的含量超过一定值后,材料的冲击强度有所下降;控制注塑时的模具温度,可以改变材料的一些力学性能。     

玻璃微珠改性PBT复合材料的制备与性能

研究了玻璃微珠(GB)、短玻纤(GF)用量对聚对苯二甲酸丁二醇酯(PBT)／GF复合材料熔体流变性和力学性能的影响。结果表明:在GF质量分数为17．5％以下时,添加GB使熔体的MFR增大,反之则减小;加工工艺对熔体的粘度也有影响。在未添加GB情况下,随CF用量增加,复合材料的拉伸、弯曲强度、弯曲模量均增大,添加GB后三者增加较缓慢;而复合材料的冲击强度在添加、未添加GB的情况下均减小;添加GB后成型试样的表面更光洁。     

Compatibility of softwood flour and commercial biopolymers in injection molding

This study is focused on wood flour‐reinforced biopolymers for injection molding. Eight commercial biopolymers were compounded with 30 and 50% wood flour and injection molded. Thermal processability via extrusion was evaluated by use of the resulting melt pressure, melt temperature, and machine load, during injection molding the injection pressure was taken. Clear increases of melt‐ and injection pressures could be determined at rising fiber load and better shaping of the molded parts was observed. The mechanical performance of the composites and the neat polymers was evaluated by tensile‐, bending‐, and impact properties. To study the effects of different fiber concentrations, multiple comparison tests were calculated. High variations in the mechanical properties and in hygroscopic behavior were found between the different biopolymers. Through incorporation of wood flour, the E‐modules of all polymers were significantly improved. The strength values of the various biopolymers offered different trends because of the reinforcement. The polylactic acid (PLA) and the cellulose‐based polymer Biograde showed significant decreases in strength by addition of wood flour. Scanning electron micrographs of a 50% filled PLA compound revealed low fiber matrix adhesion. Impactstrength and elongation at yield of all investigated polymers dropped dramatically with rising fiber content. POLYM. COMPOS., 2010. © 2009 Society of Plastics Engineers     

树脂传递模塑工艺中工艺参数对树脂-纤维界面的影响

本文系统研究了工艺参数对由树脂传递模塑成型的复合材料的拉伸强度和树脂-纤维界面的影响.这些参数包括注射压力和模腔/纤维毡的温度.在较低的注射压力和较高的成型温度下,纤维得到良好的浸润和粘结,成型复合材料的拉伸强度也较高.     

Microcellular Foamed Wood‐Plastic Composites by Different Processes: a Review

Wood fiber reinforced polymer composites represent a relatively small but rapidly growing material class, extensively applied in interior building applications and in the automotive industry. The polymer‐wood fiber composites utilize fibers as reinforcing filler in the polymer matrix and are known to be advantageous over the neat polymers in terms of the materials cost and mechanical properties such as stiffness and strength. Wood fiber reinforced polymer composites are microcellularly processed to create a new class of materials with unique properties. Most manufacturers are evaluating new alternatives of foamed composites that are lighter and more like wood. Foamed wood composites accept screws and nails like wood, more so than their non‐foamed counterparts. They have other advantages such as better surface definition and sharper contours and corners than non‐foamed profiles, which are created by the internal pressure of foaming. This paper represents a review on microcellular wood fiber reinforced polymer composites obtained by different processes (batch, injection molding, extrusion, and compression molding process) and includes an overview of foaming agents (physical and chemical) and the foaming of wood fiber‐polymer composites (changes in phase morphology, formation of polymer‐gas solution, cell nucleation, and cell growth control).